HUG
Geneva, Canton of Geneva, 1205, Switzerland
Location status: Recruiting
NCT Number: NCT05066412
To assess safety of prophylactic escaladed dose of T naïve depleted (CD45RA depleted donor lymphocyte infusion, in patients with malignant hemopathie who received an allogeneic stem cell transplant from an haplo-identical donor, after a reduced intensity conditionning regiment.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 1
Geneva, Canton of Geneva, 1205, Switzerland
Location status: Recruiting
Primary Objective is to determine whether the administration of prophylactic CD45RAneg (CD45RAneg) memory/effector T lymphocytes is feasible and safe in the early post-transplant period for patients with haploidentical transplant and RIC conditioning.
Donor lymphocytes are isolated from the original donor by non-mobilized mononuclear cell leukapheresis. Repetitive intravenous infusions (up to 3) of escalating doses of CD45RAneg cells, prepared from the leukapheresis by CliniMACS® technology (CD45RA-depletion), storage in vapor nitrogen.
Escalating doses of CD45RAneg cells, for patients with haploidentical graft, intervals of 6-8 weeks, if GvHD is absent starting ≥ 4 weeks from the day of transplantation.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
CD45RAneg cells, prepared from mononuclear cell leukapheresis by CliniMACS® technology
Time frame: 24 hours after each CD45RA neg DLI infusion
acute transfusion reaction after each DLI infusion (CTCAE ≥ 2)
Time frame: within 8 weeks after each CD45RAneg DLI infusion
acute GvHD grade II-IV measured with MAGIC score
Contact information is provided by the study sponsor or research team.
University Hospital, Geneva
Other
A Phase I Clinical Trial Assessing Prophylactic Donor CD45RA-depleted Lymphocyte Infusions Into Patients Transplanted with Stem Cell Grafts from Haploidentical Donors After Reduced Intensity Conditioning
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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